TELMIS
Manage your clinical trials efficiently
TELMIS, your tool for managing controlled clinical trials
TELMIS is the CTMS solution designed to provide those involved in clinical research with administrative data and manage study-related documents. From planning to coordinating centers, TELMIS makes every step of the process more efficient and secure.
Developed by industry professionals, the platform meets the operational requirements of academic, industrial and institutional sponsors, integrating regulatory standards and best practices in the field.
With TELMIS, you'll be able to conduct your clinical studies efficiently and focus on what's most important: the quality and success of your projects.
TELMIS is an all-in-one solution that simplifies and secures the management of clinical studies thanks to powerful centralized functionalities.
- Real-time planning and monitoring: its interface lets you track inclusions, visits or critical events. Customized dashboards give you an up-to-date overview of your studies;
- Center, contact and document management: TELMIS centralizes all survey center data to ensure smooth, secure management;
- Team coordination: users have personalized access, assigned tasks and action tracking to facilitate activity management.
With TELMIS, research teams can guarantee greater efficiency, transparency and control throughout the study lifecycle.
TELMIS combines technology and human support to simplify study management while guaranteeing quality and efficiency.
- Saves time: by reducing administrative burdens and automating processes, TELMIS enables research teams to focus on coordination and quality;
- Quality control and compliance: it improves the quality of studies and facilitates document traceability with data that can be used at any time;
- Human support: TELMIS is much more than just a tool. It's also a dedicated, responsive project team.
This unique combination enables teams to carry out studies more easily, with greater reliability and confidence.
Our quality commitments
